US4115476A - 2,2,6,6-Tetramethyl-4-piperidyl carbonic acid esters of dihydric alcohols and phenols as stabilizers for synthetic polymers - Google Patents

2,2,6,6-Tetramethyl-4-piperidyl carbonic acid esters of dihydric alcohols and phenols as stabilizers for synthetic polymers Download PDF

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US4115476A
US4115476A US05/794,172 US79417277A US4115476A US 4115476 A US4115476 A US 4115476A US 79417277 A US79417277 A US 79417277A US 4115476 A US4115476 A US 4115476A
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Motonobu Minagawa
Naohiro Kubota
Toshihiro Shibata
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Adeka Corp
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Argus Chemical Corp
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
    • C08K5/3432—Six-membered rings
    • C08K5/3435—Piperidines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/40—Oxygen atoms
    • C07D211/44—Oxygen atoms attached in position 4
    • C07D211/46—Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4

Definitions

  • Hindered 2,2,6,6-tetraalkyl-4-carboxylic acid ester piperidine compounds have been proposed by Murayama et al U.S. Pat. No. 3,640,928 patented Feb. 8, 1972 as light and heat stabilizers for synthetic polymers, such as polyolefins, polyvinyl chloride, polyvinylidene chloride, polyurethanes, and polyamides. These compounds have the general formula: ##STR3## or a salt thereof.
  • R 1 and R 2 which may be the same or different, each are an alkyl group such as methyl, ethyl, isopropyl or dodecyl, or they form, together with the carbon atom to which they are attached, a saturated alicyclic group such as: ##STR4## or a group of the formula ##STR5##
  • n is an integer of 1 to 3 inclusive:
  • R 3 is an acyl group.
  • the compounds generally employed previously have either been highly colored, such as the nickel compounds (which are normally green) and the 2-hydroxybenzophenones (which are varying shades and intensities of yellow). They also show very little tendency towards sublimation and exudation, and they have an excellent stabilizing action against both heat and light deterioration.
  • Murayama et al patent has been followed by a large number of patent and literature disclosures by Murayama et al. and others of compounds including a 2,2,6,6-tetrasubstituted-4-piperidyl group attached to a base molecule of varying structures.
  • R represents an alkyl group, an alkenyl group, an alkenoyl group which may be substituted with an aryl group, a hydroxyalkyl group, an alkoxyalkyl group, an alkoxycarbonylalkyl group, an acyloxyalkyl group, a cyanoalkyl group or nitroso group, and X and Y individually represent oxygen atom or sulfur atom.
  • R 1 represents hydrogen atom, an alkyl group, a substituted alkyl group, an alkenyl group, an alkynyl group, a substituted or unsubstituted aralkyl group, an aliphatic acyl group, an alkoxycarbonyl group or an aralkoxycarbonyl group, n is an integer of 1 to 4;
  • R 2 represents hydrogen atom, an aliphatic, aromatic or heterocyclic monoacyl group, an alkyl group, an alkenyl group, an alkynyl group, an aralkyl group, an aryl group, an alkoxyalkyl group, an epoxyalkyl group, an alkoxysulfonylalkyl group, N-substituted carbamoyl group, a N-substituted thiocarbamoyl group, a monovalent group from an oxoacid or group ##STR8## in which
  • R 3 represents hydrogen atom, a lower alkyl group or phenyl group and R 4 represents an alkyl group;
  • R 2 represents carbonyl group, an aliphatic or aromatic diacyl group, an alkylene group, an alkenylene group, an alkynylene group, an aralkylene group, a N-substituted dicarbamoyl group or a divalent group from an oxoacid;
  • R 2 represents an aromatic triacyl group or a trivalent group from an oxoacid
  • R 2 represents an aromatic tetraacyl group
  • A represents a group ##STR9## in which
  • R 3 represents hydrogen atom or a lower alkyl group or, when n is 1, R 5 may represent together with R 2 a group ##STR10## in which
  • R 6 represents the same group as defined in R 1 and may be the same or different from R 1 , or a group ##STR11## in which
  • n and m are 1 or 2 and R 7 represents hydrogen atom or, when n and m are 1, R 7 represents methylene group together with R 2 .
  • R' represents an alkyl group, a substituted alkyl group, an acyl group, an alkoxycarbonyl group, a substituted alkoxycarbonyl group, an amino group, a substituted amino group or nitroso group;
  • X represents oxygen atom or sulfur atom
  • Y represents oxygen atom, sulfur atom or a group of the formula ⁇ N--R" in which R" is hydrogen atom, an alkyl group or a substituted alkyl group;
  • Z represents oxygen atom or a group of the formula >N--R''' is hydrogen atom, an alkyl group or a substituted alkyl group;
  • n is an integer of 1 through 4 inclusive
  • R represents, when n is 1, an alkyl group, a substituted alkyl group, an aryl group, a substituted aryl group, a cycloalkyl group, an alkoxycarbonyl group, a substituted alkoxycarbonyl group, a substituted phosphino group or a substituted phosphinyl group, when n is 2, an alkylene group, an alkenylene group, an arylene group, a substituted arylene group, an aralkylene group, an alkylenediphenylene group, a bis-(acyloxyalkylene) group, an alkylene-bis-(oxycarbonylalkyl) group, a dialkylene ether group or a diphenylene ether group, when n is 3, an alkanetriyl group, a tris(acyloxyalkylene) group, an alkane-tris-(oxycarbonylalkyl) group or a group of the group ##STR13## in
  • n is an integer of 1 through 8 inclusive, and when n is 4, an alkane tetrayl group, a tetrakis-(acyloxyalkylene) group or an alkanetetrakis(oxycarbonylalkyl) group.
  • n is an integer of 1 or 2 and X is an alkylene group, or o-, m- or p-phenylene group or the carbon atoms of CO groups may be directly joined in the absence of X or a group of the formula: ##STR15## in which
  • Y is an alkylene group or o-, m- or p-phenylene group.
  • R 1 and R 2 are methyl or together with the carbon to which they are bound form a mono-cyclic ring system having five or six carbon atoms;
  • R 3 is an alkyl group of from one to twenty atoms
  • R 4 is hydrogen or methyl
  • m 0 or 1.
  • R 1 and R 2 are independently of each other methyl or ethyl or together with the carbon to which they are bound form a cyclopentyl or cyclohexyl ring, which is unsubstituted or substituted with a methyl group;
  • n is an integer of from 1 to 2;
  • R 3 is an alkyl group of from one to 20 carbon atoms
  • R 3 is an alkylene group of from two to eight carbon atoms
  • A is a straight or branched chain (lower) alkylene group containing from one to six carbon atoms with the limitation that the terminals of said alkylene group bear only hydrogen or one (lower) alkyl group.
  • R 1 and R 2 independently of each other are straight- or branchedchain alkyl having from one to six carbon atoms, or together with the carbon to which they are bound form a cyclopentyl or cyclohexyl ring, which is unsubstituted or substituted with a methyl group;
  • R 3 is hydrogen, alkyl having one to twelve carbon atoms, ⁇ -methoxyethyl, alkenyl having three or four carbon atoms, propargyl, benzyl or alkyl-substituted benzyl;
  • R 4 is straight or branched-chain alkylene having five to eight carbon atoms, or the group (CH 2 ) m Y(CH 2 ) n wherein Y is oxygen or sulfur and m and n independently of each other are an integer from 1 to 3;
  • M is hydrogen or a metal selected from the group consisting of barium, nickel, manganese, calcium, zinc, iron, sodium, cobalt, tin, and dialkyl tin, and
  • z has a value of from 1 to 4, the value of z being the same as the available valence of M.
  • X is S, SO or SO 2 and Y and Y 1 are the same or different and each is H, OH, O-- or a straight- or branched alkyl residue having from one to four carbon atoms, and salts thereof when Y and Y 1 are other than O---
  • R 1 and R 2 are the same or different and each is a straight-or branched alkyl residue having from one to twelve carbon atoms, or R 1 and R 2 , together with the carbon atom to which they are attached, form a cycloakyl residue having from five to twelve carbon atoms or the group: ##STR21## wherein
  • R 1 and R 2 have their previous significance and Y is a straight- or branched alkyl reside having from one to twenty carbon atoms, an alkenyl or alkynyl residue having from three to twenty carbon atoms, an aralkyl residue having from seven to twelve carbon atoms or the group --CH 2 X wherein X is the group ##STR22## wherein
  • R 3 is hydrogen, a methyl or phenyl residue, the group ##STR23## wherein
  • R 4 is an alkyl residue having from 1 to 20 carbon atoms.
  • Cook U.S. Pat. No. 3,929,804 patented Dec. 30, 1975 discloses 4-piperidine acetamide compounds having the formula: ##STR24## wherein
  • R 1 and R 2 are the same or different and each is a straight- or branched alkyl residue having from one to 12 carbon atoms, or R 1 and R 2 , together with the carbon atom to which they are attached form a cycloalkyl group having from five to 12 carbon atoms;
  • R 3 is hydrogen, a straight- or branched alkyl residue having from one to four carbon atoms, an aralkyl residue having from seven to nine carbon atoms or a cycloalkyl group having from five or six carbon atoms;
  • R 4 is a metal ion or a hydrocarbyl residue having from two to twenty carbon atoms and being either unsubstituted or substituted by halogen or interrupted by one or more oxygen or sulphur atoms;
  • X is --0--, --S--, or >NR 5 , wherein R 5 has the same significance as R 3 ;
  • n 2, 3 or 4;
  • R 7 is hydrogen, alkyl or phenyl.
  • 2,2,6,6-tetramethyl-4-piperidyl carbonic acid esters of dihydric alcohols and phenols are provided, useful as stabilizers for organic polymeric materials, having the general formula: ##STR26## wherein:
  • R 3 is selected from the group consisting of hydrogen and O;
  • R 6 is lower alkyl
  • n is selected from the group consisting of 1, 2, 3, 4 and 5;
  • --O--Z--0-- is a bivalent aliphatic, cycloaliphatic, aromatic, or mixed aliphatic-aromatic, aliphatic-cycloaliphatic or cycloaliphatic-aromatic radical carrying two hydroxyl groups OH esterified with carbonic acid groups of the piperidyl carbonic acid ester.
  • the R 6 alkyl has from one to about six carbon atoms. Exemplary are methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tertiary butyl, secondary butyl, n-amyl, isoamyl, tertiary amyl, n-hexyl, isohexyl, secondary hexyl and tertiary hexyl.
  • the Z radical has from two to about twenty-four carbon atoms in an open chain or cyclic saturated or ethylenically unsaturated structure, or mixed open chain substituted cyclic saturated or ethylenically unsaturated structure.
  • exemplary are ethylene, propylene, butylene, pentylene, hexylene, octylene, nonylene, decylene, dodecylene, tetradecylene, hexadecylene, octadecylene, cyclopentylene, cyclohexylene, cycloheptylene, ethylidene, 2,2,6,6-tetraethylene cyclohexylene, 1-hydroxyl-2,2,6,6-tetraethylene cyclohexylene, and can include ether --O--and thioether--S--linking groups between alkylene groups as in polyoxyalkylene and polythioalkylene groups having from one to about five
  • the Z arylene have from six to 24 carbon atoms and include phenylene, naphthylene and phenanthrylene.
  • the mixed Z alkcycloalkylene and cycloalkylene have from about four to about twenty-four carbon atoms, and include methylcyclohexylene, dibutyl cyclohexylene, ethyl cyclopentylene, trimethyl cyclobutylene, cyclopentane dimethylene; cycloheptane dimethylene; cyclohexane diemthylene; cyclohexane dipropylene; cyclopentane diethylene; and cyclohexane dibutylene.
  • the Z arylene and alkarylene have from seven to about twenty-four carbon atoms, and include benzene dimethylene; xylylene; 2,2-diphenyl isopropylidene; phenethylene, ethylphenylene, propylphenylene, butylphenylene, tolylene, phenpropylene, phenbutylene, naphthethylene and ethylnaphthylene.
  • Exemplary dihydric alcohols and phenols from which the Z radical is derived include ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, butylene glycol, pentanediol, hexanediol, neopentylglycol, thiodiethylene glycol, cyclohexane dimethanol, phenyldimethanol, hydrogenated Bisphenol A, cyclohexanediol hydroquinone, 2,5-di-t-butylhydroquinone, 2,3,6-trimethylhydroquinone, 2-methylresorcinol; 2,6-di-t-butylresorcinol; 2,2'-methylene-bis-(4-methyl-6-t-butylphenol); 2,2'-methylene-bis-(4-methyl-6( ⁇ -methylcyclohexyl)phenol); 2,2'-n-butylidene-bis-(4,6-di-methylphenol), bis
  • the compounds in accordance with the invention are readily prepared using conventional procedures.
  • the starting materials are either available or readily syntehsized without difficulty.
  • the corresponding 2,2,6,6-tetrasubstituted-4-hydroxy piperidine is used as a starting material for the 2,2,6,6-tetrasubstituted-4-piperidyl groups R 1 , R 2 . This is reacted optionally in the presence of an organic solvent, diphenyl carbonate, an alkaline catalyst and the corresponding dihydric alcohol or phenol.
  • the alkaline catalyst can be any alkaline catalyst conventionally employed for transesterification reactions, such as an alkali or alkaline earth metal oxide or hydroxide or an alkaline salt of an alkali or alkaline earth metal, such as carbonate, or hydride, or alcoholate.
  • Sodium is quite satisfactory, and so are sodium hydroxide, lithium carbonate, sodium carbonate, potassium carbonate, lithium hydroxide, potassium hydroxide, sodium hydride, lithium hydride, potassium hydride, calcium hydride, the oxides and hydroxides of calcium, strontium and barium, and the alcoholates, usually of methyl, ethyl or isopropyl alcohol, or phenolates of all of these metals.
  • the hydroxy group of the piperidine becomes esterified with the carbonate and alcohol or phenol forming the 4-piperidinyl carbonic acid ester of the invention: ##STR29##
  • 2,2,6,6-tetramethyl-4-hydroxy-piperidine 7.8 g (0.05 mole), diphenylcarbonate 10.7 g (0.05 mole), hydrogenated Bisphenol A 6.0 g (0.025 mole) and potassium carbonate 0.02 g were reacted at 140° C. for 3 hours under nitrogen. Then, phenol was distilled off at up to 170° C. maximum temperature for 1.5 hours under reduced pressure. A colorless glassy solid was obtained with a softening temperature of 45°-50° C.
  • the 2,2,6,6-tetrasubstituted-4-piperidyl carbonic acid esters of the invention are effective stabilizers to enhance the resistance to deterioration due to heat and/or light of synthetic polymeric materials which are susceptible to such degradation, including polyolefins such as low density polyethylene, high density polyethylene, polypropylene, polybutylene, polyisobutylene, polypentylene, and polyisopentylene; polystyrene; polydienes, such as polybutadiene and polyisoprene; and copolymers of olefins and dienes with other ethylenically and acetylenically unsaturated monomers, such as ethylene-propylene copolymers, ethylene-butene copolymers, ethylene-pentene copolymers, ethylenevinyl acetate copolymers, styrene-butadiene copolymers, acrylonitrile-styrenebutadiene
  • the synthetic polymer can be in any physical form, including (for example) filaments, yarns, films, sheets, molded articles, latex, and foam.
  • the piperidyl carbonic acid esters of the invention can be used as a stabilizer in an amount within the range from about 0.01 to about 5 parts by weight, preferably from 0.05 to 3 parts by weight, per 100 parts by weight of resin.
  • the stabilizers of the invention can be employed as the sole stabilizer or, preferably, in combination with other conventional heat and light stabilizers for the particular synthetic polymer.
  • polyvinyl chloride resins other polyvinyl chloride resin heat stabilizers can be included, including polyvalent metal fatty acid salts such as barium and cadmium salts of the higher fatty acids; organic triphosphites; organotin compounds; hindered phenols; and epoxy compounds.
  • polyolefin resins there can be employed fatty acid salts of polyvalent metals, orgaic phosphites, phenolic and thiophenolic antioxidants, and the higher fatty alcohol esters of thiodipropionic acids, such as, for example, dilauryl thiodipropionate.
  • polyamide stabilizers such as copper salts in combination with iodides and/or phosphorus compounds and salts of divalent manganese can be used.
  • antioxidants such as hindered phenols and bis-phenols, polyvalent metal salts of the higher fatty acids, and organic phosphites can be used.
  • additives for synthetic polymers such as plasticizers, lubricants, emulsifiers, antistatic agents, flameproofing agents, pigments and fillers, can be employed.
  • a group of polyvinyl chloride resin compositions was prepared having the following formulation:
  • This formulation was blended and sheeted off on a two-roll mill to form sheets 1 mm thick.
  • the light resistance of these sheets was then determined by placing strips 1 cm wide in a Weather-O-Meter, and exposing them to ultraviolet light. The time in hours was then noted for the sheets to develop a noticeable discoloration and/or embrittlement, indicating deterioration due to oxidation in the presence of ultraviolet light.
  • Polypropylene compositions were prepared using stabilizers of the invention and two of the prior art, and having the following formulation:
  • compositions were thoroughly blended in a Brabender Plastograph, and then compression-molded to form sheets 0.5 mm thick. Pieces 2.5 cm square were cut off from the sheets and exposed to a carbon arc in a Weather-O-Meter for 350 hours. Elongation before and after 350 hours exposure was determined in comparison with two controls, 2-(2'-hydroxy-5'-chlorophenyl) benzotriazole and bis (9-aza-8,8,10,10-tetramethyl-3-ethyl-1,5-dioxaspiro (5,5)-3-undecyl methyl sebacate, and the percent of retention of elongation is shown in Table II.
  • the compounds of the invention are superior stabilizers in enhancing the resistance of the polypropylene polymer composition to deterioration in the presence of ultraviolet light.
  • Ethylene-vinyl acetate copolymer compositions were prepared using stabilizers of the invention and two of the prior art, and having the following formulation:
  • the stabilizer was blended with the polymer on a two-roll mill at 130° C., and sheets 0.4 mm thick were then compression-molded at 140° C. from the resulting blend. Pieces 2.5 cm square were cut off from the sheets and exposed to ultraviolet light in a Weather-O-Meter for 500 hours. At the start and at the conclusion of the test, tensile strength of the sheet samples was determined. The results in comparison with two controls, 2-hydroxy-4-methoxy benzophenone and bis (2,2,6,6-tetramethyl-4-piperidinyl) adipate, are given in Table III as % retention of the initially determined tensile strength:
  • the stabilizer compositions in accordance with the invention are superior to 2-hydroxy-4-methoxy benzophenone and bis (2,2,6,6-tetramethyl-4-piperidinyl) adipate in enhancing the resistance of the ethylene-vinyl acetate copolymer to deterioration in the presence of ultraviolet light.
  • High density polyethylene compositions were prepared using the stabilizers of the invention and two of the prior art, and having the following formulation:
  • the stabilizer was blended with the polymer on a two-roll mill and sheets 0.5 mm thick were prepared by compression-molding of the blend. Pieces 2.5 cm square were cut off from the sheets, and exposed in a Weather-O-Meter to ultraviolet light. The time in hours when degradation set in, as determined by a significant discoloration and/or embrittlement, was noted as hours to failure, and the results are reported in Table IV:
  • the stabilizers of the invention are clearly superior to the controls in enhancing resistance of the polyethylene to degradation under ultraviolet light.
  • acrylonitrile-butadiene-styrene terpolymer resin compositions were prepared using stabilizers of the invention and two of the prior art, and having the following formulations:
  • the stabilizer was blended with the resin on a two-roll mill, and sheets 3 mm thick were prepared by compression molding of the resulting blend. Pieces 2.5 cm square were cut off from the sheets, and subjected to ultraviolet light in a Weather-O-Meter for 800 hours. Tensile strength before and after the test exposure was determined, and the results reported as the percent of tensile strength retained, at the end of this time, in Table V.
  • Polybutylene terephthalate resin formulations were prepared having the following composition:
  • compositions were extruded to form pellets, and then test pieces were molded from the pellets by injection molding at 270° C.
  • the test pieces were irradiated with ultraviolet light for 500 hours in a Weather-O-Meter.
  • Tensile strength before and after exposure was determined, and the percent tensile strength retained after the exposure is given in Table VI.
  • the stabilizers of the invention are effective ultraviolet light stabilizers for polybutylene terephthalate resins.
  • Polyurethane resin compositions were prepared using stabilizers of the invention and having the following formulation:
  • the stabilizer was blended with the finely powdered polyurethane resin on a two-roll mill for five minutes at 70° C., and the sheet was then compression-molded at 120° C. for 5 minutes to form sheets 0.5 mm thick. Pieces 2.5 cm square were cut out from the sheets, and exposed to ultraviolet light in a Weather-O-Meter for thirty hours. At the conclusion of the test period, the color of the sheets was noted. The results are given in Table VII.
  • the stabilizers of the invention are clearly superior to the controls in enhancing resistance of the polyurethane resin to degradation under ultraviolet light.

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  • Chemical & Material Sciences (AREA)
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  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Hydrogenated Pyridines (AREA)
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US05/794,172 1976-05-19 1977-05-05 2,2,6,6-Tetramethyl-4-piperidyl carbonic acid esters of dihydric alcohols and phenols as stabilizers for synthetic polymers Expired - Lifetime US4115476A (en)

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Cited By (15)

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EP0022997A1 (en) * 1979-07-12 1981-01-28 ADEKA ARGUS CHEMICAL CO., Ltd. 2,2,6,6-Tetramethyl-4-piperidyl carboxylic acid esters and amides of mono and poly alcohols, phenols and amines and synthetic polymer compositions stabilized thereby
US4250313A (en) * 1980-02-01 1981-02-10 Argus Chemical Corp. Process for preparing 4-piperidone spiroketal compounds
US4250312A (en) * 1979-12-28 1981-02-10 Argus Chemical Corp. Process for preparing 4-piperidone spiroketal compounds
EP0027620A1 (en) * 1979-10-11 1981-04-29 ADEKA ARGUS CHEMICAL CO., Ltd. 2,2,6,6-Tetraalkyl-4-piperidyl-bis-spiro-ethers and synthetic polymers stabilised therewith
EP0032566A1 (en) * 1980-01-16 1981-07-29 American Cyanamid Company Isopropylidenedicyclohexylene esters and their use as light stabilizers
US4323684A (en) * 1979-08-08 1982-04-06 Naohiro Kubota Process for preparing a 2,2,6,6-tetraalkyl-4-piperidyl spiro aliphatic ether
US4351915A (en) * 1980-05-30 1982-09-28 Adeka Argus Chemical Co., Ltd. 2,2,6,6-Tetramethyl-4-piperidyl spiro aliphatic ethers as stabilizers for synthetic polymers
JPS58160333A (ja) * 1982-03-18 1983-09-22 Toa Nenryo Kogyo Kk 耐変色性ポリオレフイン組成物
EP0108993A1 (en) * 1982-11-01 1984-05-23 ADEKA ARGUS CHEMICAL CO., Ltd. Oligomers of 2,2,6,6-tetramethylpiperidinol, polycarboxylic acid esters and synthetic polymer compositions
EP0219331A3 (en) * 1985-10-11 1988-10-05 Ici Americas Inc. Tartrate-based compound useful as stabilizers for polymers
EP0219333A3 (en) * 1985-10-11 1988-10-12 Ici Americas Inc. Oligomeric malonates, useful as light stabilizers for plastics
EP0465379A1 (fr) * 1990-07-03 1992-01-08 Rhone-Poulenc Chimie Composés à fonction pipéridinyle et leur utilisation dans les polymères
US5162405A (en) * 1987-12-24 1992-11-10 Elf Atochem North America, Inc. Single-functional and mixtures of multi-functional oligomeric performance additive compositions and their uses
US5496875A (en) * 1993-07-16 1996-03-05 Ciba-Geigy Corporation Derivatives of 2,2,6,6-tetramethyl-4-piperidinol for use as light stabilizers, heat stabilizers and oxidation stabilizers for organic materials
CN107709522A (zh) * 2015-08-07 2018-02-16 Dic株式会社 液晶组合物和使用其的液晶显示元件

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WO2017018153A1 (ja) * 2015-07-24 2017-02-02 Dic株式会社 安定剤化合物、液晶組成物および表示素子
CN107614477B (zh) * 2015-09-11 2021-08-24 株式会社艾迪科 化合物、潜伏性添加剂和含有该添加剂的组合物

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EP0022997A1 (en) * 1979-07-12 1981-01-28 ADEKA ARGUS CHEMICAL CO., Ltd. 2,2,6,6-Tetramethyl-4-piperidyl carboxylic acid esters and amides of mono and poly alcohols, phenols and amines and synthetic polymer compositions stabilized thereby
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EP0027620A1 (en) * 1979-10-11 1981-04-29 ADEKA ARGUS CHEMICAL CO., Ltd. 2,2,6,6-Tetraalkyl-4-piperidyl-bis-spiro-ethers and synthetic polymers stabilised therewith
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EP0032566A1 (en) * 1980-01-16 1981-07-29 American Cyanamid Company Isopropylidenedicyclohexylene esters and their use as light stabilizers
US4250313A (en) * 1980-02-01 1981-02-10 Argus Chemical Corp. Process for preparing 4-piperidone spiroketal compounds
US4351915A (en) * 1980-05-30 1982-09-28 Adeka Argus Chemical Co., Ltd. 2,2,6,6-Tetramethyl-4-piperidyl spiro aliphatic ethers as stabilizers for synthetic polymers
JPS58160333A (ja) * 1982-03-18 1983-09-22 Toa Nenryo Kogyo Kk 耐変色性ポリオレフイン組成物
EP0108993A1 (en) * 1982-11-01 1984-05-23 ADEKA ARGUS CHEMICAL CO., Ltd. Oligomers of 2,2,6,6-tetramethylpiperidinol, polycarboxylic acid esters and synthetic polymer compositions
EP0219331A3 (en) * 1985-10-11 1988-10-05 Ici Americas Inc. Tartrate-based compound useful as stabilizers for polymers
EP0219333A3 (en) * 1985-10-11 1988-10-12 Ici Americas Inc. Oligomeric malonates, useful as light stabilizers for plastics
US5162405A (en) * 1987-12-24 1992-11-10 Elf Atochem North America, Inc. Single-functional and mixtures of multi-functional oligomeric performance additive compositions and their uses
EP0465379A1 (fr) * 1990-07-03 1992-01-08 Rhone-Poulenc Chimie Composés à fonction pipéridinyle et leur utilisation dans les polymères
FR2664275A1 (fr) * 1990-07-03 1992-01-10 Rhone Poulenc Chimie Nouveaux composes a fonction piperidinyle et leur utilisation dans les polymeres.
US5124380A (en) * 1990-07-03 1992-06-23 Rhone-Poulenc Chimie Stabilized organic polymer compositions containing compound containing a piperidinyl group and a carbonate group
US5496875A (en) * 1993-07-16 1996-03-05 Ciba-Geigy Corporation Derivatives of 2,2,6,6-tetramethyl-4-piperidinol for use as light stabilizers, heat stabilizers and oxidation stabilizers for organic materials
CN107709522A (zh) * 2015-08-07 2018-02-16 Dic株式会社 液晶组合物和使用其的液晶显示元件

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